# Loratadine

NDC: 30142-984
Generic name: Loratadine
Labeler / Manufacturer: KROGER COMPANY
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, CHEWABLE
Routes: ORAL
Marketing started: 20210402

FDA application: ANDA210088

## Active ingredients

- LORATADINE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"30142-984"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=30142-984
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f5fbfb52-197c-437c-8977-23bd7f2ac7bd